Python library to parse, format, validate, normalize, and map sequence variants according to HGVS Nomenclature (https://hgvs-nomenclature.org/).

non-redundant, compressed, journalled, file-based storage for biological sequences

Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets

provides common tools and lookup tables used primarily by the hgvs and uta packages

Lightweight, portable variation registration and retrieval

OpenAPI-based REST interface to biological sequences and sequence metadata

Robotics Variation Automation and Scalable Testing

The code provides a collection of functions for various statistical calculations, including sorting, frequency analysis, mean calculations, and dispersion measures.

Variation Nodes for ComfyUI automation workflows | https://www.scuffedepoch.com | https://www.oragenai.com |ORAGEN TEAM

Script for generating randomized exams with questions and answers randomization using LaTeX and Python.

biocommons website, deployed to Read the Docs

This QGIS plugin creates vector layers that work with magnetic variation.

NextFlow pipelines and Python scripts for comprehensive analyses of proteomes data, providing: Clustering via MMseqs2; Labelling, filtering and aggregation of clusters; Alignments and Variation analyses; Meta clustering comparisons